Elena Parrini

10PUBLICATIONS
103CO-AUTHORS
NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Labour, migration and developmentCancer geneticsHaematological tumours
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Publications (10)

|Aug 22, 2026
A Novel Constitutional TUBB Variant Associated With Familial Malformations of Cortical Development.

|Mar 31, 2026
Genetic Etiologies of Epilepsies With Status Epilepticus: Insights From the Italian Pediatric Status Epilepticus Group Cohort.

Carla Marini, Anna Rosati, Lucia Fusco

|Oct 25, 2025
Clinical and genetic landscape of epilepsies with absence seizures and single-gene etiology.

Simona Balestrini, Ilaria Galli, Maria Luisa Ricci

|Jul 22, 2025
Development and Adaptive Function in Individuals With SCN2A-Related Disorders.

Beatrice Southby Goad, Jill Rodda, Meagan Allen

|Aug 30, 2024
Endocrinological features and epileptic encephalopathy in COX deficiency due to SCO1 mutations: case series and review of literature.

Alessandro Barbato, Giulia Gori, Michele Sacchini

|Oct 08, 2023
Bilateral temporal lobe dysplasia and seizure onset associated with biallelic CNTNAP2 variants.

Norman Panza, Claudia Bianchini, Valentina Cetica

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Frequent Collaborators

9 joint publications

Renzo Guerrini

6 joint publications

Davide Mei

3 joint publications

Carla Marini

3 joint publications

Simona Balestrini